Automated inline preparation and degassing of volatile samples for inline analysis

ABSTRACT

An analysis system includes a degassing cell, at least one first valve, and at least one second valve. The at least one first valve is fluidly coupled with a top of the degassing cell, the at least one first valve configured selectably connect the degassing cell to a displacement gas flow and to a vacuum source. The at least one second valve is fluidly connected with a lateral side of the degassing cell and separately fluidly connected with a bottom of the degassing cell. The at least one second valve is selectably coupled with any of a source of a sample-carrying fluid, a transfer line configured to deliver a sample to an analysis device, or a waste output.

BACKGROUND

In many laboratory settings, it is often necessary to analyze a large number of chemical or biological samples at one time. In order to streamline such processes, the manipulation of samples has been mechanized. Such mechanized sampling can be referred to as autosampling and can be performed using an automated sampling device, or autosampler.

Inductively Coupled Plasma (ICP) spectrometry is an analysis technique commonly used for the determination of trace element concentrations and isotope ratios in liquid samples. ICP spectrometry employs electromagnetically generated partially ionized argon plasma which reaches a temperature of approximately 7,000 K. When a sample is introduced to the plasma, the high temperature causes sample atoms to become ionized or emit light. Since each chemical element produces a characteristic mass or emission spectrum, measuring the spectra of the emitted mass or light allows the determination of the elemental composition of the original sample.

Sample introduction systems may be employed to introduce the liquid samples into the ICP spectrometry instrumentation (e.g., an Inductively Coupled Plasma Mass Spectrometer (ICP/ICP-MS), an Inductively Coupled Plasma Atomic Emission Spectrometer (ICP-AES), or the like), or other sample detector or analytic instrumentation for analysis. For example, a sample introduction system may withdraw an aliquot of a liquid sample from a container and thereafter transport the aliquot to a nebulizer that converts the aliquot into a polydisperse aerosol suitable for ionization in plasma by the ICP spectrometry instrumentation. The aerosol is then sorted in a spray chamber to remove the larger aerosol particles. Upon leaving the spray chamber, the aerosol is introduced into the plasma by a plasma torch assembly of the ICP-MS or ICP-AES instruments for analysis.

DRAWINGS

The Detailed Description is described with reference to the accompanying figures.

FIGS. 1-6 are a series of environmental views illustrating a process by which a sample carrier fluid can first form bubbles that can agglomerate and potentially form voids within tubing associated with an analysis system.

FIG. 7 is an environmental view of an analysis system designed to minimize bubble formation within a sample carrier fluid, in accordance with an example embodiment of the present disclosure.

FIGS. 8-12 are a series of environmental views of the analysis system of FIG. 7 , displaying a process by which the analysis system can be used to minimize bubble formation within tubing associated therewith.

DETAILED DESCRIPTION

Overview

In various analysis systems, a transfer fluid, such as ammonium hydroxide (NH₄OH), can be used as a transfer solution to convey a sample from a loop inlet to a waste loop or nebulizer. In an embodiment, the transfer fluid can be 29% NH₄OH. The solution can still be under pressure, and, if an analysis is started right away without waiting for the sample to depressurize, the plasma can be extinguished. Depressurization can cause the NH₄OH to flow to waste or nebulizer, depending on the valve position.

The example analysis system 1000 shown in FIGS. 1-6 can help to illustrate an issue that can arise with the development of bubbles and/or voids. The analysis system 1000 can include a loop inlet 1010, a tubing 1020 (shown straight for ease of illustration but which may, for example, be in the form of a loop of tubing), and a loop outlet 1030, which may be in the form of, for example, a nebulizer and/or a waste loop. The tubing 1020 can be configured to receive and facilitate the transmission of a sample-carrying fluid S2 (e.g., sample material carried in a carrier fluid, such as NH₄OH) therethrough. While waiting for the depressurization, many tiny bubbles 1040 (e.g., diameter less than half the diameter of the tubing 1020) can form on the sides of the tubing 1020 extending between the loop inlet 1010 and the loop outlet 1030 (e.g., in the form of a waste loop and/or a nebulizer).

As can be seen in FIG. 1 , when beginning depressurization, no bubbles 1040 may exist in the tubing 1020. Per FIG. 2 , at the start of the analysis the sample S2 can be stable with some bubbles 1040 forming, yet no or substantially no bubbles 1040 are able to make it into the nebulizer and/or the ICPMS. In an embodiment, as shown in FIG. 3 , depressurization can be expected to be finished after approximately two minutes, with a sample flow (e.g., 100 μL/min) then beginning in the tubing 1020. As can be seen from FIGS. 4 , some of the small bubbles 1040 can get pushed together by the flow in the small-diameter tubing 1020 and start to form larger bubbles 1050 (e.g., larger than the small bubbles 1040 and possibly of a diameter greater than half the diameter of the tubing 1020). Per FIGS. 5 and 6 , eventually enough bubbles 1040 and/or 1050 may push together to form a void 1060 in the liquid sample S2.

The void 1060 can be defined as a lack of sample fluid within the tubing 1020 that extends the full diameter of the tubing 1020. In an embodiment, the void 1060 may be in the form of a gas pocket within the tubing 1020. As this void 1060 gets pushed down the line, it can grow as it adds more bubbles 1040, 1050 (as particularly illustrated in FIG. 6 ) and/or other voids 1060 to itself. In some embodiments, there may be about 5-6 of these large voids 1060 in the loop or flow path section 1020 at a given time. Considering such issues, an approach is needed for degassing a sample at a remote position to deter bubbles from agglomerating to form voids within the transport tubing.

Example Implementations

Referring generally to FIGS. 7 through 12 , an example analysis system 100 configured to degas a sample at a remote position and to thereby deter bubbles from agglomerating to form voids is shown and described. The analysis system 100, as seen in FIG. 7 , can generally include at least one first valve 102 (e.g., a first multi-port valve, per the illustrated embodiment, which may be a V5-P3 valve), at least one second valve 104 (e.g., a second multi-port valve, per the illustrated embodiment, which may be a V4-P6 valve), at least one third valve 106 (e.g., a third multi-port valve, per the illustrated embodiment, which may be a V3-P3 valve), a vacuum pump 108, a manifold 110, a degassing cell 112 (e.g., a pillar tee connector, per the illustrated embodiment, with two longitudinally-spaced fluid connect ports and a lateral fluid connect port), a sample inlet 114, at least one waste outlet 116 (e.g., 116A, 116B), a plurality of fluid lines 118 (e.g., piping, tubes, etc.) to fluidly connect the various elements together, and a central analysis device (not shown) for testing the prepared sample-carrying fluid. In an embodiment, the vacuum pump 108 and the first waste outlet 116A are coupled with the manifold 110. The vacuum pump 108 can be fluidly coupled with the at least one first valve 102 via a first fluid line 118A. The system 100 can further include a degassing cell 112 (e.g., a ¾ inch pillar tee) oriented to define a top cell extension 112A, a bottom cell extension 112B, and a lateral cell extension 112C (i.e., the three connective portions associated with the degassing cell 112). The lateral cell extension 112C can extend from a side of the degassing cell 112 at a location between the top cell extension 112A and the bottom cell extension 112B. The portion of the analysis system 100 prior to the central analysis device (not shown) may also be considered to be a fluid transfer system. In an embodiment, the fluid transfer system can be a remote sample preparation and delivery system.

The at least one first valve 102 can be fluidly coupled with the top cell extension 112A of the degassing cell 112 via a second fluid line 118B (i.e., an upper fluid connect, relative to the degassing cell 112). The at least one first valve 102 can be configured to selectably connect the degassing cell 112 to a displacement gas flow or to a vacuum source. The degassing cell 112 can be separately and selectably coupled with the at least one second valve 104 using a third fluid line 118C (i.e., a lateral, central fluid connect, relative to the degassing cell 112), via the lateral cell extension 112C, and using a fourth fluid line 118D (i.e., a lower fluid connect, relative to the degassing cell 112), via the bottom cell extension 112B. The at least one second valve 104 can be fluidly coupled with the sample inlet 114 and with the at least one third valve 106 (e.g., the latter connection via a fifth fluid line 118E). The at least one second valve 104 can be selectably coupled with at least one of a source of a sample-carrying fluid, a transfer line configured to deliver a sample to an analysis device, or a second waste output. The second waste outlet 116B can be selectably connected to the at least one third valve 106, used to create a selectable fluid connection with the at least one second valve 104. In an embodiment, the at least one first valve 102, the at least one second valve 104, and/or the at least one third valve 106 may, respectively, be in the form of a multiport valve, per the illustrated embodiment. In an embodiment, the at least one first valve 102, the at least one second valve 104, and/or the at least one third valve 106 used herein may be, for example, pneumatically and/or electrically controlled and/or may be in a form of a distribution manifold. In an embodiment, the at least one first valve 102, the at least one second valve 104, and/or the at least one third valve 106 can also be in the form of mass flow controllers (MFC's) capable of electronically selectable flow control therethrough. In an embodiment, the at least one first valve 102, the at least one second valve 104, and/or the at least one third valve 106 can be in the form of a plurality of valves (e.g., instead of, for example, a corresponding multi-port valve).

The operation of the analysis system 100 is illustrated in FIGS. 8-12 , in accordance with an embodiment of the present disclosure. With respect to FIG. 8 , a sample flow 120 (e.g., a sample material in a carrier fluid (e.g., a carrier fluid including ammonium hydroxide and/or another volatile component) is directed into the bottom cell extension 112B and, thereby, through the degassing cell 112. The sample flow 120 (i.e., sample-carrier fluid) can reach the bottom cell extension 112B via the sample inlet 114, the at least one second valve 104, and the fourth fluid line 118D. With further respect to FIG. 8 , the at least one first valve 102 can be configured to selectably direct a flow of nitrogen gas (i.e., N₂) or another inert gas, functioning as a displacement gas, into the top cell extension 112A via the second fluid line 118B, resulting in an amount of N₂ or other displacement gas being trapped under pressure at a top of the degassing cell 112. In an embodiment, the displacement gas and the pressure provided thereby can prevent and/or retard the sample-carrier fluid from flowing beyond the top cell extension 112A and toward the at least one first valve 102.

In the situation presented in FIG. 8 , the vacuum pump 108 is not fluidly connected to the degassing cell 112 (e.g., via the at least one first valve 102), and the sample flow 120 exiting the degassing cell 112 via its lateral cell extension 112C can ultimately be directed to the second waste outlet 116B via the second and at least one third valves 104, 106. That is, the influx of fluids (e.g., nitrogen/inert gas and sample flow) through the top and bottom of the degassing cell 112 can dictate that some or all such fluids be driven out through the lateral cell extension 112C (i.e., the only available escape/release location). In an embodiment, the degassing cell 112 can be filled partially or fully with the sample-carrying fluid before the displacement gas is introduced into the degassing cell 112. In an embodiment, the flow of the displacement gas may be increased to help force any sample-carrying fluid lying at or above third fluid line 118C out of the degassing cell 112 and ultimately toward the waste outlet 116B associated with the at least one third valve 106.

In a second step, as illustrated in FIG. 9 , the flow connections remain the same, except the sample flow 120 is turned off, with the N₂ or other displacement gas flow continuing. The continued flow of nitrogen increases the pressure on the sample remaining in the degassing cell 112, pushing any of the sample lying at or above the third fluid line 118C from the degassing cell 112 and to waste. Once the excess sample within the degassing cell 112 has been pushed to waste, per FIG. 9 , the flow combination illustrated in FIG. 10 can then be activated. In the situation of FIG. 10 , the sample flow 120 from the sample inlet 114 remains off, the flow through at least one third valve 106 is opened toward an analysis device (not labelled) and no longer flowing through the second waste outlet 116B. Further, per FIG. 10 , the N₂/displacement gas flow is disconnected, with the degassing cell 112 being subjected to a vacuum via the vacuum pump 108 via the at least one first valve 102, with the fluid pulled through the vacuum pump 108 directed to the first waste outlet 116A.

FIG. 11 maintains the flow connections set forth in FIG. 10 , showing the results thereof. The flow mechanics prompted by the vacuum can cause all the liquid to be removed from the fourth fluid line 118D and the ammonia gas (NH3) and/or another gas (e.g., ammonium hydroxide or other volatile component) to be removed from the sample flow 120. Due to the vacuum, the sample flow 120 can actively bubble during the conditions of FIG. 11 , and the degassing cell 112 can feel cold during this step (e.g., as part of the heat exchange associated with the ammonia and/or other gas evaporation).

Finally, per the step illustrated in FIG. 12 , the degassing cell 112 can be reconnected with the flow of N₂/displacement gas (e.g., via the first or at least one second valves 102, 104), disconnected from the vacuum flow, and disconnected from the at least one third valve 106. Additionally, flow to a transfer line 122 to a central analysis device (not shown) can be opened at the at least one second valve 104. As a result, the pressure from the N₂/displacement gas flow can push the sample, now carrying no or substantially no ammonia/ammonium hydroxide and/or other volatile component (at least not enough to generate any voids), as a sample flow 120 through the fourth fluid line 118D, into the at least one second valve 104, and into the transfer line 122. The portion of the system 100 capable of delivering to the transfer line 122 and the central analysis device may be considered to be a remote flow handling system.

In an embodiment, upon loading the sample into the analysis system 100, the ammonium hydroxide sample can be properly degassed in about seven (7) minutes before transferring the sample for analysis. In some embodiments, after degassing, there was found to be no need to permit the sample to rest in the loop, as opposed to a situation without degassing. Other samples incorporating other volatile substances may take a different length of time to degas. Without degassing, the sample must be permitted to rest in the loop to keep the ICPMS plasma on in cool plasma. Upon using the present system to degas the ammonium hydroxide sample, no noticeable voids may be seen in the analysis loop after transfer. Upon degassing, some small NH₄OH and/or NH₃ bubbles may still form but at a level so as not to appear to affect testing (i.e., substantially all ammonia is removed prior analysis, at least to a point where the remaining ammonia/ammonium hydroxide remaining does not interfere with testing), at which point the sample can be considered sufficiently degassed. In an embodiment, an upgrade kit for transfer remotes using two valves and a vacuum pump is within the scope of this present system, with all parts able to mount to the existing blanks on the remote fluid handling system.

In an embodiment, the analysis system 100 (e.g., implemented as an upgrade kit) may be used for thinner samples or with other samples where degassing may prove necessary (e.g., not just with ammonia-based samples but, for example, when any potentially volatile (i.e., high vapor pressure) sample carrier is employed). In an embodiment, it is to be understood that the present system may be used with any analysis system where degassing of the sample may prove necessary to deter void formation. In an embodiment, a suitable gas (e.g., an inert gas) may be used as the displacement gas, in place of nitrogen in the embodiment discussed herein. In some embodiments, the sample may be heated (e.g., prior to entry into the analysis system 100 and/or at the degassing cell 112) to promote degassing. In an embodiment, the sample can be cooled at the receiving point of the central, particularly if the sample is expressly heated to promote degassing.

In embodiments, a system controller (not shown) can be available for controlling the operation of the analysis system 100 (e.g., valve and/or vacuum operation; and/or any related flow inputs). The system controller can include a processor, a memory, and a communications interface. In an embodiment, the analysis system 100 can include one or more sensors (e.g., flow sensors, pressure sensors, etc.) able to work in conjunction with the system controller, as needed to achieve the desired functionality of the system. The processor provides processing functionality for at least the controller and can include any number of processors, micro-controllers, circuitry, field programmable gate array (FPGA) or other processing systems, and resident or external memory for storing data, executable code, and other information accessed or generated by the controller. The processor can execute one or more software programs embodied in a non-transitory computer readable medium that implement techniques described herein. The processor is not limited by the materials from which it is formed or the processing mechanisms employed therein and, as such, can be implemented via semiconductor(s) and/or transistors (e.g., using electronic integrated circuit (IC) components), and so forth.

The memory can be an example of tangible, computer-readable storage medium that provides storage functionality to store various data and or program code associated with operation of the controller, such as software programs and/or code segments, or other data to instruct the processor, and possibly other components of the system 100, to perform the functionality described herein. Thus, the memory can store data, such as a program of instructions for operating the system 100 (including its components), and so forth. It should be noted that while a single memory is described, a wide variety of types and combinations of memory (e.g., tangible, non-transitory memory) can be employed. The memory can be integral with the processor, can comprise stand-alone memory, or can be a combination of both.

Some examples of the memory can include removable and non-removable memory components, such as random-access memory (RAM), read-only memory (ROM), flash memory (e.g., a secure digital (SD) memory card, a mini-SD memory card, and/or a micro-SD memory card), magnetic memory, optical memory, universal serial bus (USB) memory devices, hard disk memory, external memory, remove (e.g., server and/or cloud) memory, and so forth. In implementations, memory can include removable integrated circuit card (ICC) memory, such as memory provided by a subscriber identity module (SIM) card, a universal subscriber identity module (USIM) card, a universal integrated circuit card (UICC), and so on.

The communications interface can be operatively configured to communicate with components of the system 100. For example, the communications interface can be configured to transmit data for storage by the system 100, retrieve data from storage in the system 100, and so forth. The communications interface can also be communicatively coupled with the processor to facilitate data transfer between components of the system 100 and the processor. It should be noted that while the communications interface is described as a component of controller, one or more components of the communications interface can be implemented as external components communicatively coupled to the system 100 or components thereof via a wired and/or wireless connection. The system 100 or components thereof can also include and/or connect to one or more input/output (I/O) devices (e.g., via the communications interface), such as a display, a mouse, a touchpad, a touchscreen, a keyboard, a microphone (e.g., for voice commands) and so on.

The communications interface and/or the processor can be configured to communicate with a variety of different networks, such as a wide-area cellular telephone network, such as a cellular network, a 3G cellular network, a 4G cellular network, a 5G cellular network, or a global system for mobile communications (GSM) network; a wireless computer communications network, such as a WiFi network (e.g., a wireless local area network (WLAN) operated using IEEE 802.11 network standards); an ad-hoc wireless network, an internet; the Internet; a wide area network (WAN); a local area network (LAN); a personal area network (PAN) (e.g., a wireless personal area network (WPAN) operated using IEEE 802.15 network standards); a public telephone network; an extranet; an intranet; and so on. However, this list is provided by way of example only and is not meant to limit the present disclosure. Further, the communications interface can be configured to communicate with a single network or multiple networks across different access points. In a specific embodiment, a communications interface can transmit information from the controller to an external device (e.g., a cell phone, a computer connected to a WiFi network, cloud storage, etc.). In another specific embodiment, a communications interface can receive information from an external device (e.g., a cell phone, a computer connected to a WiFi network, cloud storage, etc.).

Although the subject matter has been described in language specific to structural features and/or methodological acts, it is to be understood that the subject matter defined in the appended claims is not necessarily limited to the specific features or acts described above. Rather, the specific features and acts described above are disclosed as example forms of implementing the claims. 

1.-20. (canceled)
 21. A fluid transfer process for a sample-containing fluid, comprising: providing a flow of a sample-carrying fluid into a degassing cell provided in a location remote from a sample analysis device; fluidically connecting the degassing cell with a vacuum source to generate a vacuum pressure in the degassing cell, the vacuum pressure promoting a degassing of the sample-carrying fluid to provide a degassed sample-carrying fluid; after degassing the sample-carrying fluid, supplying a transfer fluid to the degassing cell to push the degassed sample-carrying fluid to a transfer line fluidically coupled between the degassing cell and the analysis device for transfer to the analysis device.
 22. The fluid transfer process of claim 21, wherein the degassing cell defines a top cell extension, a bottom cell extension, and a lateral cell extension, the lateral cell extension extending from a side of the degassing cell at a location between the top cell extension and the bottom cell extension.
 23. The fluid transfer process of claim 21, further comprising, prior to fluidically connecting the degassing cell with the vacuum source, introducing a flow of a displacement gas into the degassing cell.
 24. The fluid transfer process of claim 23, wherein introducing a flow of a displacement gas into the degassing cell occurs simultaneously with providing the flow of the sample-carrying fluid into the degassing cell.
 25. The fluid transfer process of claim 23, the transfer fluid is the displacement gas.
 26. The fluid transfer process of claim 21, wherein the sample-carrying fluid comprises ammonium hydroxide, and wherein a gas comprising at least one of ammonium hydroxide or ammonia is degassed therefrom upon application of the vacuum pressure.
 27. A fluid transfer system, comprising: a degassing cell configured to promote degassing of a sample-carrying fluid prior to transfer from a remote sample system to a sample analysis device; a valve system fluidically coupled with the degassing cell; one or more computer processors; and a non-transitory computer readable-medium bearing one or more instructions for execution by the one or more computer processors to cause the one or more computer processors to perform the steps of: providing a flow of a sample-carrying fluid into a degassing cell provided in a location remote from the sample analysis device; fluidically connecting the degassing cell with a vacuum source via the valve system to generate a vacuum pressure in the degassing cell, the vacuum pressure promoting a degassing of the sample-carrying fluid to provide a degassed sample-carrying fluid; after degassing the sample-carrying fluid, supplying a transfer fluid to the degassing cell via the valve system to push the degassed sample-carrying fluid to a transfer line fluidically coupled between the degassing cell and the analysis device for transfer to the analysis device.
 28. The fluid transfer system of claim 27, wherein the degassing cell defines a top cell extension, a bottom cell extension, and a lateral cell extension, the lateral cell extension extending from a side of the degassing cell at a location between the top cell extension and the bottom cell extension.
 29. The fluid transfer system of claim 27, wherein the non-transitory computer readable-medium further includes one or more instructions for execution by the one or more computer processors to cause the one or more computer processors to perform the steps of: prior to fluidically connecting the degassing cell with the vacuum source, introducing a flow of a displacement gas into the degassing cell.
 30. The fluid transfer system of claim 29, wherein introducing a flow of a displacement gas into the degassing cell occurs simultaneously with providing the flow of the sample-carrying fluid into the degassing cell.
 31. The fluid transfer system of claim 29, the transfer fluid is the displacement gas.
 32. The fluid transfer system of claim 29, wherein the sample-carrying fluid comprises ammonium hydroxide, and wherein a gas comprising at least one of ammonium hydroxide or ammonia is degassed therefrom upon application of the vacuum pressure. 